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CV Bank — Human Resources

Reference Number: 000001574
Posted Date: 11/25/2021
Closing Date: 12/10/2021

Department: LTRI, Zane Cohen Center
Position: Clinical Trials Coordinator I

POSITION TITLE  Clinical Trials Coordinator I
EMPLOYMENT TYPE Temporary Part Time
HOURS OF WORK  22.5  hours per week
REPORTS TO  Principal Investigator


The Lunenfeld-Tanenbaum Research Institute of Mount Sinai Hospital, a University of Toronto affiliated research center, is one of the world's leading centers in biomedical research.  With groundbreaking discoveries in research areas such as diabetes, genetic disorders, cancer, and women's and infants' health, the Institute is committed to excellence in health research and the training of young investigators.  Strong partnerships with the clinical programs of Mount Sinai Hospital ensure that scientific knowledge is used to promote human health.  Your significant contributions will assist in maintaining our momentum in advancing our research.


  • Support of research activities related to Dr. Targownik's IBD clinic and research program.
  • Support of the clinical activities of the IBD clinic and research program.
  • The successful candidate will have excellent organizational skills and will be able to work well within the context of an interdisciplinary clinical and research team.
  • He/she will have solid communication skills, be very detail-oriented, and works independently when the need arises.
  • The successful candidate will work under the direction of Dr. Targownik and in collaboration with the clinical and research members of Dr. Targownik's IBD clinic and research program.
  • A background in medical/clinical/health data skills would be an asset.



The Clinical Research Coordinator I collaborates with Investigators and the health care team to assume responsibility for the overall study participant management and coordination of several clinical studies. The Clinical Research Coordinator I will work primarily in the prospective and retrospective research studies. Studies include pharma sponsored as well as Investigator-initiated trials.

Responsibilities include:

  • Assisting in maintaining the clinical and research registries of IBD patients
  • Data abstraction from participants' chart
  • Recruitment of study participants (e.g., identify and screen potential subjects, obtain informed consent)
  • Coordination of study participant visits schedules as per study protocol
  • Providing clinical communication to study participants according to the study protocol and the implementation and coordination of all aspects of data collection and source documentation, as per SHS policy and ICH/GCP guidelines
  • Identifying and consenting of research participants for research studies
  • Liaising with patients and coordinating patient scheduling or facilitating such visits




  • Undergraduate degree in a health-related discipline
  • 1-2 years of relevant experience (e.g., epidemiology, economics, data science, statistics) is an asset
  • Nursing Degree or Physician's Assistant Degree with interest in clinical research is an asset
  • Background in clinical trials or prior research experience, desirable
  • Experience in a clinical healthcare environment and/or a clinical research setting
  • Excellent computer skills and an ability to learn and comprehend the technical requirements
  • Proficient in utilizing Microsoft Office programs such as Excel, Word, PowerPoint, and Access is required
  • General knowledge of clinic scheduling systems and clinic work-flow
  • Effective verbal and written communication skills, interpersonal and client service skills
  • Excellent organization and time management skills
  • Demonstrate ability to communicate effectively with physicians, clinical team members, administrative and research staff
  • Ability to maintain confidentiality exercises discretion, work independently, and commits to excellence

In accordance with Institute's policy and legislated health and safety requirements, employment is conditional upon the verification of credentials, completion of a health review, and demonstrating proof of immunity and vaccination status of vaccine-preventable diseases. All employees and affiliates will follow safe work practices and comply with health and safety policies, procedures, and training. Successful candidates will be required to provide two (2) written reference letters from their former employer(s)/supervisor(s).

To ensure the safety and wellbeing of all our people and patients, Sinai Health has made it a priority to support everyone in getting vaccinated against COVID-19. Consistent with this, our Staff Immunization & Surveillance Policy was recently updated to include the requirement for full vaccination – currently defined as receiving two doses and serving a 14-day waiting period following the second dose – in order to be able to work at Sinai Health. To be compliant with our updated Policy, you must provide proof of dual COVID-19 vaccination, as indicated on the Prospective Immunization and Surveillance Policy Information Sheet, in order to be eligible for employment at Sinai Health. If you believe you are one of the very few people who may require an exemption from vaccination, supporting medical information must be submitted to our Occupational Health department, who will review and assess.


We are a fully committed to fairness and equity in employment and our recruitment and selection practices. We encourage applications from Indigenous peoples, people with disabilities, members of sexual minority groups, members of racialized groups, women and any others who may contribute to the further diversification of our Sinai Health community. Accommodation will be provided in all parts of the hiring process as required under our Access for People with Disabilities policy. Applicants need to make their requirements known in advance.



Posting open until Decemebr 10, 2021 We thank all candidates for applying. Only those selected for an interview will be contacted.

Hours: 22.5 hours to 24 hours per week

Contact Name: Online


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